VarSome Insights makes patient recruitment faster, cheaper, and more targeted by starting at the variant level.

Support your outreach and clinical programs: starting from the genetic variant

varsome_insights-1Genetically supported drug targets can significantly increase the chances of approval. If you have a genetic biomarker, VarSome Insights can make it faster, cheaper, and more efficient to find patients based on molecular profile.

Let us show you how


Leverage VarSome's global community of over 500 000 professionals. is home to one of the world's most comprehensive databases of human genome variant information. Clinicians across six continents use to classify and interpret genetic variants to support diagnoses.

Over 87% of VarSome users have consented to have their information shared for relevant clinical studies or approved therapies. VarSome Insights allows you to see which clinicians have been investigating your genes of interest, including their:

  • Job title
  • Organization
  • Location
  • Gene and Variant search
  • Variant classification
  • Email address

Key benefits


Get your message to the right audience gets over 500 000 page views per month by Healthcare Professionals across six continents, allowing you to get your message in front of your target audience.

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Locate candidates and sites

Use VarSome search data to track disease prevalence and find clinicians with relevant patients. 

A global community

Work in real-time with information from one of the world's largest communities of clinical geneticists and connect with them to support your clinical programs.


Start the conversation

With more than 87% of the users consenting to be contacted about relevant trials and therapies, you can reach out to healthcare professionals in your target regions.

How we can support you

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Retrospective data

A detailed report of search activity on your gene of interest, for the past two years. This can be used to measure prevalence and find recent potential clinical cases

Active reports

Subscribe to weekly reports of search activity on your gene of interest. This helps you identify active clinical cases before the diagnosis has taken place.

Live outreach

The VarSome Insights team can reach out to relevant clinicians on your behalf. Confirming the presence of a patient, make them aware of your study, and make introductions towards study enrolment.

Native advertisements

Insert your content into relevant result pages for your genes of interest, promoting a clinical study, approved therapy, or raising awareness.  

Some words from our partners


1.Successful clinical trial enrolment

"We had another person agree to participate in our clinical trial. That's a great record of success."


2.Rare disease awareness

"We look forward to leveraging Saphetor's innovative approach to bring together the global genomics community to build awareness in our rare disease program."


3.Disease prevalence mapping

"Traditional prevalence efforts are usually a costly and timely endeavor. Inferred prevalence may circumvent this spend during early development efforts."

Interested in supporting your clinical programs?

Let us know how we can help